Ectopic sebaceous glands of Gibsan in eyelid margin– A novel manifestation in Stevens Johnson Syndrome & proposed nomenclature based on an observational case series

2020 ◽  
Vol 18 (3) ◽  
pp. 523-525 ◽  
Author(s):  
Geetha Iyer ◽  
Bhaskar Srinivasan ◽  
Shweta Agarwal ◽  
Krishnakumar Subramanian
Author(s):  
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Dinesh Kansal ◽  
Usha Chaudhary ◽  
Ajay Sharma ◽  
Reena Sharma

2021 ◽  
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pp. 915-918
Author(s):  
Laura LY Hui ◽  
Celine Loke ◽  
Derrick CW Aw ◽  
Liesbet Tan ◽  
Lie Michael George Limenta ◽  
...  

2018 ◽  
Vol 35 (3) ◽  
pp. 392-396 ◽  
Author(s):  
Taru Garg ◽  
Sarita Sanke ◽  
Riaz Ahmed ◽  
Ram Chander ◽  
Srikanta Basu

PEDIATRICS ◽  
2007 ◽  
Vol 119 (4) ◽  
pp. e1002-e1005 ◽  
Author(s):  
K. A. Ravin ◽  
L. D. Rappaport ◽  
N. S. Zuckerbraun ◽  
R. M. Wadowsky ◽  
E. R. Wald ◽  
...  

2021 ◽  
Vol 65 ◽  
pp. 51-54
Author(s):  
Bhavana Srivastava ◽  
Reena Bhardwaj ◽  
Renu Khanchandani ◽  
Zafar Masood Ansari ◽  
Gunjita Belwal

Stevens-Johnson syndrome (SJS) is a rare, serious disorder and may be life threatening affecting mainly mucocutaneous tissues. It is a type of generalised, multisystemic hypersensitivity reaction directly linked to the drug intake. It is one of the few serious adverse effects of drugs involving skin and mucous membranes which are characterised by rash, bullae and blisters spread on skin, mucous membranes, swelling with erosive lesions on lips and face and hyperpigmentation. Normally, SJS is a self-resolving condition but it has potential to be converted into life-threatening disease. Here, we describe and present a case series of SJS inflicted by rifampicin and allopurinol. First one is a 28-year-old-female and second case is a 50-year-old male, both received rifampicin for pulmonary tuberculosis. Third patient is a 22-year-old young male taken allopurinol for hyperuricemia. All these patients noticed a severe skin reaction which is a part of erythema multiforme spectrum. Causality assessment was done in these patients with the help of Naranjo’s algorithm and diagnosed as cases of SJS.


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